ENST00000454293.2:c.*29+2310T>G
|
ENSP00000412014.2:n.*29+2310T>G
|
|
ENST00000463153.2:c.306+2310T>G
|
|
|
ENST00000644371.2:c.*2339T>G
MANE Select
|
ENSP00000495778.1:n.*2339T>G
|
|
ENST00000649763.1:c.*29+2310T>G
|
ENSP00000497701.1:n.*29+2310T>G
|
|
ENST00000463153.1:n.309+2310T>G
|
|
|
NM_016006.4:c.*2339T>G
|
NP_057090.2:n.*2339T>G
|
|
XM_011533779.1:c.*2339T>G
|
XP_011532081.1:n.*2339T>G
|
|
XM_011533780.1:c.*2365T>G
|
XP_011532082.1:n.*2365T>G
|
|
XR_940447.1:n.3334T>G
|
|
|
NM_001355186.1:c.*29+2310T>G
|
NP_001342115.1:n.*29+2310T>G
|
|
NM_001365649.1:c.*2339T>G
|
NP_001352578.1:n.*2339T>G
|
|
NM_001365650.1:c.*2365T>G
|
NP_001352579.1:n.*2365T>G
|
|
NM_016006.5:c.*2339T>G
|
NP_057090.2:n.*2339T>G
|
|
NR_158560.1:n.3400T>G
|
|
|
NM_001355186.2:c.*29+2310T>G
|
NP_001342115.1:n.*29+2310T>G
|
|
NM_016006.6:c.*2339T>G
MANE Select
|
NP_057090.2:n.*2339T>G
|
|